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Infant acute respiratory distress syndrome
1 OMIM reference -
2 associated genes
21 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital pulmonary alveolar proteinosis
Chronic respiratory distress with surfactant metabolism deficiency
Desquamative interstitial pneumonia
Idiopathic pulmonary fibrosis
Neonatal acute respiratory distress with surfactant metabolism deficiency
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Joubert syndrome
Joubert syndrome with hepatic defect
Meckel syndrome
Progressive non-fluent aphasia
Semantic dementia
Senior-Boichis syndrome
Spastic paraplegia - Paget disease of bone
Hamel cerebro-palato-cardiac syndrome
X-linked intellectual deficit, Golabi-Ito-Hall type
X-linked intellectual deficit, Porteous type
X-linked intellectual deficit, Sutherland-Haan type
- Hyaline membrane disease
- Infant ARDS
- Infant respiratory distress syndrome
- Neonatal respiratory distress syndrome

Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
- Certain conditions originating in the perinatal period -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
SFTPB P07988178640
SFTPC P11686178620
No signs/symptoms info available.